THINPREP 2000 SYSTEM (UDI P950039)
Manufactured by Hologic, Inc.
Device Regulatory Overview
The THINPREP 2000 SYSTEM (Model/Catalog Number: Unspecified) is a medical device manufactured by Hologic, Inc.. This product is indexed under FDA Product Code / Category Classification MKQ within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- MKQ
- Device Name
- Processor, cervical cytology slide, automated
- Database Sync Date
- 2026-08-09 10:04:44
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of THINPREP 2000 SYSTEM?
The registered manufacturer of record for THINPREP 2000 SYSTEM is Hologic, Inc..
What is the Primary UDI-DI identifier for THINPREP 2000 SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P950039.
What classification code is assigned to this device?
This device is registered under product classification code MKQ.
Similar Classification Devices (MKQ)
Other Devices by Hologic, Inc.
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